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Functional Annotations of Novel Cancer-Associated lncRNAs Identified Using Machine Learning Algorithms

机译:使用机器学习算法识别的新型癌症相关lncRNA的功能注释

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Cancer consists of a set of diseases that result from deregulated cell growth and invasion of adjacent tissues. Due to an increase in research, more information has become available regarding the potential causes for cancer, including non-coding elements such as lncRNAs. This new knowledge can be discovered through machine learning methods that can extract new information from data such as gene expression profiles and identify new cancer-associated genes. For this work we use two different machine learning algorithms, random forests and support vector machines. The models were trained and we tested fine-tuning methods including: balancing and feature selection. The predictors with the highest metrics were: balanced RF with Boruta (AUC-ROC: 0.9696) and the balanced SVM with recursive feature elimination (AUC-ROC: 0.9710). These models were used to identify new potential lncRNA driver-like genes from protein coding expression data. The predicted candidates were then functionally annotated using disease ontologies and molecular function ontologies to determine their enrichment in cancer related processes. These processes included prostate cancer and glycosaminglycan binding, a potential tumor therapeutic target.
机译:癌症由一系列因细胞生长失调和邻近组织浸润引起的疾病组成。由于研究的增加,关于癌症的潜在原因(包括非编码元件,如lncRNA)的更多信息已变得可用。可以通过机器学习方法发现这种新知识,机器学习方法可以从诸如基因表达谱等数据中提取新信息,并识别与癌症相关的新基因。对于这项工作,我们使用两种不同的机器学习算法,即随机森林和支持向量机。对模型进行了训练,我们测试了微调方法,包括:平衡和特征选择。度量最高的预测变量是:具有Boruta的平衡RF(AUC-ROC:0.9696)和具有递归特征消除的平衡SVM(AUC-ROC:0.9710)。这些模型被用来从蛋白质编码表达数据中鉴定出新的潜在的lncRNA司机样基因。然后使用疾病本体和分子功能本体在功能上注释预测的候选对象,以确定它们在癌症相关过程中的富集程度。这些过程包括前列腺癌和糖氨糖聚糖结合,这是潜在的肿瘤治疗靶标。

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